Affiliations: [a] Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Alzheimer Center Limburg, Maastricht University, Maastricht, Netherlands
| [b] Department of Neurology, Alzheimer Center, VU University Medical Center, Amsterdam, Netherlands
Correspondence:
[*]
Correspondence to: Stephanie J.B. Vos, Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Alzheimer Center Limburg, Maastricht University, P.O. Box 616, 6200 MD Maastricht, the Netherlands. Tel.: +31433881036; E-mail: [email protected].
Abstract: Increasing interest in clinical trials and clinical research settings to identify Alzheimer’s disease (AD) in the earliest stages of the disease has led to the concept of preclinical AD. Individuals with preclinical AD have AD pathology without clinical symptoms yet. Accumulating evidence has shown that biomarkers can identify preclinical AD and that preclinical AD is associated with a poor clinical outcome. Little is known yet about the role of vascular and lifestyle risk factors in the development of preclinical AD. In order to better understand preclinical AD pathology and clinical progression rates, there is a need to refine the concept of preclinical AD. This will be of great value for advancements in future research, clinical trials, and eventually clinical practice.
